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A novel magnetically recoverable palladium nanocatalyst containing organoselenium ligand for the synthesis of biaryls via Suzuki-Miyaura coupling reaction

机译:一种新型磁力可恢复的钯纳米催化剂,含有有机烯配体,用于通过Suzuki-miyaura偶联反应合成芳烃

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摘要

In the present work, a novel heterogeneous catalytic system involving palladium(II) complex as moisture- and air-stable organoselenium ligand supported on Fe3O4 nanoparticles modified by SiO2/azidopropyltriemethoxy silane was designed, synthesized and characterized using various physicochemical methods inclusive VSM, EDX, FE-SEM, TG, XRD, and FT-IR spectroscopy. The catalytic activity of the synthesized magnetic nanocatalyst which named Fe3O4@SiO2-T-Se/Pd(II) was evaluated in Suzuki-Miyaura coupling reactions for the preparation of corresponding biaryls using diverse aryl halides and arylboronic acids. The mild reaction conditions, variety of substrate scope, good yield, low reaction time, high stability, utilization of organoselenium compound as an air and moisture insensitive ligand and its immobilization on solid support, and more importantly effortless recovery and recyclability of the catalyst up to seven consecutive runs with no remarkable change in its activity are some of the interesting features of this protocol that makes it more beneficial from both industrial and environmental points of view.
机译:在本作研究中,设计了一种新的异质催化系统,其涉及钯(II)复合物作为由SiO 2 /偶氮丙基三氧乙氧基硅烷改性的Fe3O4纳米颗粒中负载的水分和空气稳定的有机烯配体进行设计,合成和表征各种物理化学方法,包括VSM,EDX, Fe-SEM,TG,XRD和FT-IR光谱。在Suzuki-Miyaura偶联反应中评价了鉴于Fe3O4 @ SiO2-T-SE / Pd(II)的合成磁性纳米催化剂的催化活性,用于使用各种芳基卤化物和芳基硼​​酸制备相应的芳基。温和的反应条件,底物范围的种类,产率良好,低反应时间,高稳定性,有机烯化合物的利用作为空气和水分不敏感配体及其固定化对固体载体的固定,更重要的是催化剂的易于努力的恢复和催化剂的可回收性。其活动中没有显着变化的连续七次运行是本协议的一些有趣功能,从工业和环境观点来看,它使其更有益。

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